We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Register to vote Register by 18 June to vote in the General Election on 4 July.
Explains how conditions attached to a planning permission should be used and discharged effectively
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Upper Tribunal Administrative Appeals Chamber decision by Judge Stout on 2 May 2024.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Employment Appeal Tribunal Judgment of Mr Justice Kerr on 23 May 2024.
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
Information about the EU Regulations and their implementation in Northern Ireland
Accrediting qualifications: how and when we do it
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Guidance on activities that may require a marine licence.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
This test requirement applies only to electrical and electronic equipment where immunity to RF (radio frequency) interference is of principal importance.
If you are not purchasing your trees from a commercial supplier, use this form to request an exception from the Biosecure Procurement requirement.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Find information and support on how to comply with the biosecure procurement requirement for suppliers of plants and trees.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).